R Winardi

Molecular basis for membrane rigidity of hereditary ovalocytosis. A novel mechanism involving the cytoplasmic domain of band 3.

Narla Mohandas, R Winardi, D. Knowles et al. · Journal of Clinical Investigation · 1992 · 147 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +17

Mechanochemistry of protein 4.1's spectrin-actin-binding domain: ternary complex interactions, membrane binding, network integration, structural strengthening.

Dennis E. Discher, R Winardi, Pierre Olivier Schischmanoff et al. · The Journal of Cell Biology · 1995 · 108 citations · Full text

Life Sciences, Biophysics, Cell Biology +17

Defining of the Minimal Domain of Protein 4.1 Involved in Spectrin-Actin Binding

Pierre Olivier Schischmanoff, R Winardi, Dennis E. Discher et al. · Journal of Biological Chemistry · 1995 · 63 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +17

An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cells.

John G. Conboy, Joel Anne Chasis, R Winardi et al. · Journal of Clinical Investigation · 1993 · 42 citations · Full text

Life Sciences, Genetics, Molecular Biology +13

Hereditary elliptocytosis due to both qualitative and quantitative defects in membrane skeletal protein 4.1

J Conboy, R Shitamoto, Mireya Parra et al. · Blood · 1991 · 39 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9